Canonical Allele Identifier: CA923726328

Gene: DDX41

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177512317C>A , CM000667.2:g.177512317C>A	GRCh38
NC_000005.9:g.176939318C>A , CM000667.1:g.176939318C>A	GRCh37
NC_000005.8:g.176871924C>A	NCBI36
NG_046846.1:g.10010G>T
NG_046846.2:g.9645G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016222.4:c.1621+5G>T MANE Select	NP_057306.2:n.1621+5G>T
ENST00000330503.12:c.1621+5G>T MANE Select	ENSP00000330349.8:n.1621+5G>T
NM_001321732.1:c.1243+5G>T	NP_001308661.1:n.1243+5G>T
NM_001321732.2:c.1243+5G>T	NP_001308661.1:n.1243+5G>T
NM_001321830.1:c.1243+5G>T	NP_001308759.1:n.1243+5G>T
NM_001321830.2:c.1243+5G>T	NP_001308759.1:n.1243+5G>T
NM_016222.2:c.1621+5G>T	NP_057306.2:n.1621+5G>T
NM_016222.3:c.1621+5G>T	NP_057306.2:n.1621+5G>T
ENST00000330503.11:c.1675+5G>T	ENSP00000330349.7:n.1675+5G>T
ENST00000503078.5:n.1914+5G>T
ENST00000505081.5:n.2488+5G>T
ENST00000507900.5:n.1125+5G>T
ENST00000507955.5:c.1621+5G>T	ENSP00000422753.1:n.1621+5G>T
ENST00000507955.6:c.1768+5G>T	ENSP00000422753.2:n.1768+5G>T
ENST00000512334.5:n.224+5G>T
ENST00000650742.1:n.1604+5G>T
ENST00000652565.1:n.736+5G>T
ENST00000652618.1:n.1618+5G>T
ENST00000652623.1:n.1693+5G>T
XM_006714870.1:c.1243+5G>T	XP_006714933.1:n.1243+5G>T
XM_024446109.1:c.1264+5G>T	XP_024301877.1:n.1264+5G>T